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DANIELLE DELUCY
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Recording
FDA Case Scenarios – Best Practices for Managing Inspection Situations
FDB2169
DANIELLE DELUCY
Duration: 75 Minutes
Add To Cart
Recording
How to conduct Annual Product Reviews to achieve GMP Compliance
FDB3164
DANIELLE DELUCY
Duration: 75 Minutes
Add To Cart
Recording
Good Documentation Practices
FDB2866
DANIELLE DELUCY
Duration: 75 Minutes
Add To Cart
Recording
Steam Sterilization Microbiology and Autoclave Performance Qualification
FDB2261
DANIELLE DELUCY
Duration: 75 Minutes
Add To Cart
Recording
Effective Batch Record Review
FDB2469
DANIELLE DELUCY
Duration: 75 Minutes
Add To Cart
Recording
3-Hour Virtual Seminar on Handling OOS Test Results and Completing Robust Investigations
FDB3384
DANIELLE DELUCY
Duration: 3 Hour
Add To Cart
Recording
Effective Standard Operating Procedure (SOPs) Development for Regulatory Compliance
FDB1868
DANIELLE DELUCY
Duration: 75 Minutes
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Recording
GMP Data Integrity – Implementation and Management
FDB1869
DANIELLE DELUCY
Duration: 75 Minutes
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Recording
Investigating Deviations – Best Practices
FDB1860
DANIELLE DELUCY
Duration: 75 Minutes
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Recording
Robust CAPA and Proper Root Cause Analysis
FDB2165
DANIELLE DELUCY
Duration: 75 Minutes
Add To Cart
Recording
How to Properly Investigate OOS Results
FDB2166
DANIELLE DELUCY
Duration: 75 Minutes
Add To Cart
Recording
How To Properly Manage a Regulatory Inspection
FDB2266
DANIELLE DELUCY
Duration: 75 Minutes
Add To Cart
Recording
How to Conduct Successful Supplier Audits
FDB2164
DANIELLE DELUCY
Duration: 75 Minutes
Add To Cart
Recording
Proper Root Cause Analysis
FDB2466
DANIELLE DELUCY
Duration: 75 Minutes
Add To Cart
Recording
Sunshine Act Reporting – Clarification for Clinical Research
FDB3162
DANIELLE DELUCY
Duration: 75 Minutes
Add To Cart
Recording
Achieving Compliance with Proper CAPA Systems
FDB2862
DANIELLE DELUCY
Duration: 60 Minutes
Add To Cart
Recording
Capturing Justifications in Change Control, Risk Assessment, Validations, and Investigations
FDB2461
DANIELLE DELUCY
Duration: 75 Minutes
Add To Cart
Recording
Successful Deviation Investigations
FDB2462
DANIELLE DELUCY
Duration: 60 Minutes
Add To Cart
Recording
Guideline to Aseptic Technique and Clean Room Behavior
FDB2463
DANIELLE DELUCY
Duration: 75 Minutes
Add To Cart
Recording
Laboratory Controls – Anticipate the Systems Based FDA Inspection
FDB2467
DANIELLE DELUCY
Duration: 75 Minutes
Add To Cart
Recording
Process Validation LifeCycle
FDB2468
DANIELLE DELUCY
Duration: 75 Minutes
Add To Cart
Recording
Conducting Successful Quality Audits
FDB2863
DANIELLE DELUCY
Duration: 75 Minutes
Add To Cart
Recording
Biosafety and Blood borne Pathogen Safety in the Lab
FDB2861
DANIELLE DELUCY
Duration: 75 Minutes
Add To Cart
Recording
Understanding Aseptic Technique and Cleanroom Behavior – Avoiding Human Error
FDB2865
DANIELLE DELUCY
Duration: 75 Minutes
Add To Cart
Recording
Successful Change Control Management
FDB2868
DANIELLE DELUCY
Duration: 75 Minutes
Add To Cart
Recording
3-Hour Virtual Seminar on Successful Deviation Investigations
FDB3081
DANIELLE DELUCY
Duration: 3 Hour
Add To Cart
Recording
Critical Elements Of Quality Risk Management Relating to FDA Compliance
FDB2262
DANIELLE DELUCY
Duration: 75 Minutes
Add To Cart
Recording
Effective Standard Operating Procedure (SOPs) Development
FDB3161
DANIELLE DELUCY
Duration: 75 Minutes
Add To Cart
Recording
Step-By-Step Process For Successful Sterility Failure Investigations
FDB2465
DANIELLE DELUCY
Duration: 75 Minutes
Add To Cart
Recording
3-Hour Virtual Seminar On Batch Record Review And Product Release
FDB3282
DANIELLE DELUCY
Duration: 3 Hour
Add To Cart
Recording
3-Hour Virtual Seminar on Handling OOS Test Results and Completing Robust Investigations
FDB3384
DANIELLE DELUCY
Duration: 3 Hour
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